Canonical Allele Identifier: PA2828053283
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1777096
ClinVar RCV Id: RCV002403589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Leu388Ser
CA16024897
NM_001354905.2:c.1163T>C